Showing posts with label hope. Show all posts
Showing posts with label hope. Show all posts

Monday, October 27, 2014

Unexpected gifts


This past weekend was filled with the unexpected. One of our favorite surprises was the warm Michigan weather that allowed our littles to play outside without coats and (for two crazy littles who couldn't be convinced otherwise) barefoot. The other favorite is shown in this picture above, seems like a fairly typical photo, but it's pretty special at the Tripped Up Castle.

Description stolen from Tripped Up Daddy's Facebook account:

Enjoying the air glider together. We've gotten close a few times earlier, but this was the first time it was initiated on its own.

Autism progress for the little Angel triplet!

This moment is brought to you through hours and hours of ABA therapy, occupational therapy, Floortime therapy, and the fantastic teachers in the ASD room. (Thanks too to the foundation provided in the ECSE programs we've used since the girls were 18 months old).

Tuesday, April 30, 2013

The Tripped Up Life celebrates 1000 Ausome Things #AutismPositivity2013

Today I'm participating in the Autism Positivity Project Flash Blog by celebrating two of the most "ausome" parts of my world: Angel and Princess triplets. This flash blog is about showing the world the positive side of autism, the acceptance part of autism. And, on the last day of Autism Awareness month, I felt it was important to participate in - even though I'm really late in the day.

Here is a description from the author of The Third Glance blog, who is one of the major organizers in this effort. I couldn't have explained it any better than this: Last year hundreds of bloggers came together in a show of support and solidarity in response to an anonymous person’s Google search “I wish I didn’t have Aspergers”. The posts that came flooding in from all over the world were a beautiful example of the power of strength in numbers. With so much negativity still surrounding Autism and the misinformation and misconceptions that continue to abound, we invite each of you to share one, or two, or more “Ausome” things! 

Princess and Angel triplets
No matter how difficult life can be when raising triplets, two of which have neurological differences which make communication extremely difficult, there's never a day without moments of pure and overwhelming love and pride in my children - all my children, those with autism and those who are neurotypical.

No matter what trouble Angel triplet has started, my heart always melts when she looks up and says, "Hi!" Just like how my heart always skips a beat whenever Princess triplet sings one of her favorite songs.

These are my awesome girls. These are my sweet, strong, and determined girls who work so hard every day just to fit in a world that doesn't really understand them. Every day they make me smile, every day they make me shake my head too, just like my other children. Every day they are my children first and little girls with autism second.

These are my "ausome," positive, hopeful, proud things that I get to shout to the world about. I have the privilege, the honor, (and yes, sometimes the struggle), the responsibility of raising these amazing autistic daughters - for that I am truly blessed.


Wednesday, December 5, 2012

The hope of babble breaks

Princess triplet surprised me yesterday when I realized her normal babble of "Princeeze" had actually broken into "I didn't do it, I didn't do it" in English. It took a second or two to realize that's a line from The Polar Express which she hasn't seen in a week or so. Rather than say this is an autistic behavior of random language usage, I'm choosing to believe she was actually asking to watch the movie. Does an out of context full sentence count as a child using sentences? Maybe not, but it does give me room for hope.

Hope is one thing I've really started to embrace in this land of special needs where I live and raise my kids. It's always a little different in families where there are kids with special needs and as parents we can often feel isolated (usually not in a good way). Lately I've been trying hard to switch my perspective on the toughest parts of the daily parenting experience of kids with autism (of preschoolers with autism, of triplets - 2 of whom seem to be in perpetual toddlerhood). Switching my perspective means looking at the things that drive me crazy, switching the lens, and choosing to see a benefit within the struggle itself. Suddenly this lens change, this change of perspective has brought me more into hope overall. It's also allowed me to see that as a special needs parent, I get to hugely celebrate the littlest milestones of my kids without anyone groaning. Nobody minds when we throw hopeful parties over here.

So yesterday's (and today's so far) hopeful party was all because of a break in babble, a break in babble into English.

And guess what? It doesn't matter how irritating that kid is in The Polar Express who repeatedly says, "I didn't do it." I can hear that from my Princess triplet for the next 2 days straight and be really excited about beginning speech patterns every single time.